US2018289003A1PendingUtilityA1

Synergistic antibacterial activity of medium polarity oils in combination with antibacterial agents on bacterial biofilms

Assignee: SMITH & NEPHEW INCPriority: Aug 24, 2015Filed: Aug 23, 2016Published: Oct 11, 2018
Est. expiryAug 24, 2035(~9.1 yrs left)· nominal 20-yr term from priority
A61K 31/7036A61K 31/085A61L 31/028A61L 29/106A61K 33/18A61K 33/38A61K 31/25A61L 31/088A61L 29/16A01N 37/02A61L 2420/04A61K 31/625A61L 27/306A61L 31/022A01N 59/12A61K 45/06A61K 47/10A61K 31/23A61L 27/34A61K 38/12A61K 9/06A61K 47/14A61K 47/26A61P 31/04A01N 59/16A61K 31/79A61K 47/38A01N 37/46A61L 2300/406A61L 27/54A61L 31/145A61L 2300/404A61L 27/025A61L 29/085A61K 9/0014A61L 31/16A61L 27/047A01N 25/30A61L 29/02A61L 29/145A61L 31/10A61L 26/0066A01N 25/04A61L 27/52Y02A50/30
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Claims

Abstract

The compositions of the present invention comprise at least one medium polarity oil and at least one antibacterial agent, the combination of which produces a synergistic antibacterial effect against bacterial biofilms. Methods are disclosed for the reduction of bacteria in and/or elimination of bacterial biofilms on biological and non-biological surfaces, as well as methods for the treatment of wounds, skin lesions, mucous membrane lesions, and other biological surfaces infected or contaminated with bacterial biofilms.

Claims

exact text as granted — not AI-modified
1 .- 114 . (canceled) 
     
     
         115 . A composition comprising a combination of at least one medium polarity oil having an octanol-water partition coefficient (log P) of 0.5 to 2.0 and at least one antibacterial agent, wherein the concentrations of the at least one medium polarity oil and the at least one antibacterial agent in the composition are at amounts that exhibit synergistic antibacterial activity against bacterial biofilms on biological and non-biological surfaces, and wherein the medium polarity oil is a glyceryl ester. 
     
     
         116 . The composition of  claim 115 , wherein the composition further comprises a pharmaceutical carrier. 
     
     
         117 . The composition of  claim 115 , wherein the antibacterial agent is not a C9-C12 aliphatic alcohol. 
     
     
         118 . The composition of  claim 115 , wherein the antibacterial agent is a silver compound, and wherein the silver compound is silver sulfadiazine, silver nitrate, or silver chloride. 
     
     
         119 . The composition of  claim 118 , wherein the composition comprises a carrier and the carrier is a ringing gel. 
     
     
         120 . The composition of any of  claim 118 , wherein the silver compound is at a concentration of 0.1 to 5% w/w. 
     
     
         121 . The composition of  claim 115 , wherein the antibacterial agent is an iodine compound, and wherein the iodine compound is an iodophor. 
     
     
         122 . The composition of  claim 121 , wherein the iodophor is cadexomer-iodine, and wherein the cadexomer-iodine is at a concentration of 40 to 60% w/w. 
     
     
         123 . The composition of  claim 121 , wherein the iodophor is povidone-iodine, and wherein the povidone-iodine is at a concentration of 1 to 20% w/w. 
     
     
         124 . The composition of  claim 115 , wherein the antibacterial agent is an antibiotic, and wherein the composition comprises a carrier and the carrier is a ringing gel. 
     
     
         125 . The composition of  claim 124 , wherein the antibiotic is an aminoglycoside antibiotic chosen from gentamicin or gentamicin sulfate, and wherein the gentamicin or gentamicin sulfate is at a concentration of 0.1 to 5% w/w. 
     
     
         126 . The composition of  claim 124 , wherein the antibiotic is a polypeptide antibiotic chosen from colistin or colistin sulfate, and wherein the concentration of colistin or colistin sulfate is 0.01 to 2% w/w. 
     
     
         127 . The composition of any of  claim 115 , wherein the glyceryl ester is glyceryl caprylate/caprate. 
     
     
         128 . The composition of  claim 127 , wherein the glyceryl caprylate/caprate is at a concentration of 7 to 40% w/w. 
     
     
         129 . The composition of  claim 115 , wherein the bacterial biofilm is a gram-positive bacterial biofilm. 
     
     
         130 . The composition of  claim 115 , wherein the bacterial biofilm is a gram-negative bacterial biofilm. 
     
     
         131 . The composition of  claim 115 , wherein the biological surface is a chronic wound, and wherein the chronic wound is a diabetic foot ulcer, venous ulcer, arterial ulcer, decubitus ulcer, stasis ulcer, pressure ulcer, or burn. 
     
     
         132 . The composition of  claim 115 , wherein the biological surface is a skin lesion, or mucous membrane lesion, and wherein the skin lesion or mucous membrane lesion, is a blister, ulceration, abrasion, wart, scrape, or infection. 
     
     
         133 . An article of manufacture comprising a surface coated with the composition of  claim 115 . 
     
     
         134 . The article of manufacture of  claim 133 , wherein the article of manufacture is a medical device. 
     
     
         135 . The article of manufacture of  claim 133 , wherein a biofilm is not present on the coated surface. 
     
     
         136 . The article of manufacture of  claim 133 , wherein a biofilm is present on the coated surface. 
     
     
         137 . A method of treating a wound, mucous membrane lesion, or skin lesion infected or contaminated with a bacterial biofilm, the method comprising topically administering to the wound, mucous membrane lesion, or skin lesion a composition of  claim 115 .

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